Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes-Reference-Cited by-同舟云学术

Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

Published:2006-07 Issue: Volume:254-255 Page:60-69
ISSN:0303-7207
Container-title:Molecular and Cellular Endocrinology
language:en
Short-container-title:Molecular and Cellular Endocrinology

Author:

Pitteloud Nelly,Meysing Astrid,Quinton Richard,Acierno James S.,Dwyer Andrew A.,Plummer Lacey,Fliers Eric,Boepple Paul,Hayes Frances,Seminara Stephanie,Hughes Viriginia A.,Ma Jinghong,Bouloux Pierre,Mohammadi Moosa,Crowley William F.

Publisher

Elsevier BV

Subject

Endocrinology,Molecular Biology,Biochemistry

Reference33 articles.

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4. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome;Dode;Nat. Genet.,2003

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